Variant report

Variant	rs13239757
Chromosome Location	chr7:41070621-41070622
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:41062800-41082200	Weak transcription	Aorta	Aorta
2	chr7:41065800-41071000	Enhancers	HMEC	breast
3	chr7:41066600-41070800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr7:41066600-41073600	Enhancers	NH-A	brain
5	chr7:41066800-41070800	Enhancers	NHEK	skin
6	chr7:41067600-41070800	Enhancers	Hela-S3	cervix
7	chr7:41067800-41071000	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr7:41068800-41071200	Weak transcription	Placenta	Placenta
9	chr7:41069200-41070800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr7:41069200-41074600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr7:41069400-41082000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr7:41069800-41072800	Weak transcription	Osteobl	bone
13	chr7:41070400-41070800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr7:41070400-41073600	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr7:41070600-41070800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr7:41070600-41073000	Weak transcription	NHDF-Ad	bronchial
17	chr7:41070600-41075200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr7:41070600-41076600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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